@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_head
{
this:
np:hasAssertion
dgn-np:NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_assertion
;
np:hasProvenance
dgn-np:NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_provenance
;
np:hasPublicationInfo
dgn-np:NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_assertion
a
np:Assertion
.
dgn-np:NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_provenance
a
np:Provenance
.
dgn-np:NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_assertion
{
miriam-gene:24
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGN200e3d9d42c9ee38de9f4c3b96aa9f84
sio:SIO_000628
miriam-gene:24
,
lld:C0242383
;
a
sio:SIO_001121
.
}
dgn-np:NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_provenance
{
dgn-np:NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_assertion
dcterms:description
"[We hypothesize that most ABCR mutations can be classified in different classes of severity, and that, depending on the remaining total activity of ABCR, the phenotype can range from AMD at the mild end to RP at the severe end of the spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:9810566
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:36+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}